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717705004: Mayer-Rokitansky-Küster-Hauser-syndroom type 2 (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3310060017 Mayer-Rokitansky-Küster-Hauser syndrome type 2 (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3310061018 Mayer-Rokitansky-Küster-Hauser syndrome type 2 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3993221011 Atypical MRKH (Mayer Rokitansky Kuster Hauser) syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3993222016 Mullerian duct aplasia, renal dysplasia, cervical somite anomalies syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6671891000146114 MURCS-associatie nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6671901000146110 syndroom van Mayer-Rokitansky-Küster-Hauser type 2 nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6671911000146112 MRKH-syndroom type 2 nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6671931000146117 atypisch MRKH-syndroom nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
10670001000146111 Mayer-Rokitansky-Küster-Hauser-syndroom type 2 nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
10670011000146113 Mayer-Rokitansky-Küster-Hauser-syndroom type 2 (aandoening) nl Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Mayer-Rokitansky-Küster-Hauser syndrome type 2 (disorder) Is a Rokitansky sequence (disorder) true Inferred relationship Some
Mayer-Rokitansky-Küster-Hauser syndrome type 2 (disorder) Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Some 1
Mayer-Rokitansky-Küster-Hauser syndrome type 2 (disorder) Occurrence Congenital true Inferred relationship Some 1
Mayer-Rokitansky-Küster-Hauser syndrome type 2 (disorder) Finding site Vaginal structure false Inferred relationship Some 1
Mayer-Rokitansky-Küster-Hauser syndrome type 2 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Mayer-Rokitansky-Küster-Hauser syndrome type 2 (disorder) Is a Malformation sequence false Inferred relationship Some
Mayer-Rokitansky-Küster-Hauser syndrome type 2 (disorder) Finding site Structure of upper third of vagina true Inferred relationship Some 1
Mayer-Rokitansky-Küster-Hauser syndrome type 2 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Mayer-Rokitansky-Küster-Hauser syndrome type 2 (disorder) Finding site Uterine structure true Inferred relationship Some 2
Mayer-Rokitansky-Küster-Hauser syndrome type 2 (disorder) Occurrence Congenital true Inferred relationship Some 2
Mayer-Rokitansky-Küster-Hauser syndrome type 2 (disorder) Finding site Structure of middle third of vagina true Inferred relationship Some 3
Mayer-Rokitansky-Küster-Hauser syndrome type 2 (disorder) Occurrence Congenital true Inferred relationship Some 3
Mayer-Rokitansky-Küster-Hauser syndrome type 2 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Mayer-Rokitansky-Küster-Hauser syndrome type 2 (disorder) Is a Congenital absence of vagina false Inferred relationship Some
Mayer-Rokitansky-Küster-Hauser syndrome type 2 (disorder) Is a Congenital absence of uterus false Inferred relationship Some
Mayer-Rokitansky-Küster-Hauser syndrome type 2 (disorder) Associated morphology Absence (morphologic abnormality) true Inferred relationship Some 1
Mayer-Rokitansky-Küster-Hauser syndrome type 2 (disorder) Associated morphology Absence (morphologic abnormality) true Inferred relationship Some 2
Mayer-Rokitansky-Küster-Hauser syndrome type 2 (disorder) Associated morphology Absence (morphologic abnormality) true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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